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家蚕响应 BmNPV 感染的 lncRNA 介导的基因调控网络分析。

Analysis of lncRNA-mediated gene regulatory network of Bombyx mori in response to BmNPV infection.

机构信息

Sericultural Research Institute, Jiangsu University of Science and Technology, Zhenjiang, China.

Sericultural Research Institute, Jiangsu University of Science and Technology, Zhenjiang, China; The Key Laboratory of Silkworm and Mulberry Genetic Improvement, Ministry of Agriculture and Rural Affairs, Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Zhenjiang, China.

出版信息

J Invertebr Pathol. 2020 Feb;170:107323. doi: 10.1016/j.jip.2020.107323. Epub 2020 Jan 9.

Abstract

Bombyx mori nucleopolyhedrosis virus (BmNPV) has always been a great challenge to the development and stability of the sericulture industry. LncRNAs have been reported to play important roles in gene expression regulation, development and immune response but the roles of lncRNAs in BmNPV infection and silkworm-BmNPV interaction are not clear. We used a genome-wide transcriptome analysis to identify the lncRNAs in Bombyx mori cells (BmN cells) and analyzed the differentially expressed lncRNAs, microRNAs and protein-coding genes in silkworm cells with or without BmNPV infection. A total of 13,159 candidate lncRNAs were identified in the BmN cells, among which 4450 lncRNAs were differentially expressed (DE) with 2837 up-regulated and 1613 down-regulated. In addition, 66 differentially expressed miRNAs (DEmiRNAs) and 7448 differentially expressed mRNAs (DEmRNAs) were identified, and DElncRNA-DEmiRNA-DEmRNA regulatory network was constructed. Gene expression was variable in 4973 of predicted lncRNA cis target genes in BmNPV infected cells. KEGG pathway analysis indicated that the target genes of DElncRNAs are enriched in ubiquitin mediated proteolysis, endocytosis and lysosome pathways. qRT-PCR validated the differential expression of several lncRNAs and miRNAs. Our results suggested that DElncRNAs participate in host response to BmNPV infection via interactions with their target genes and miRNAs. Our results will help us to improve our understanding of lncRNA-mediated regulatory roles in BmNPV infection and provide new insights into silkworm-pathogen interactions.

摘要

家蚕核型多角体病毒(BmNPV)一直是蚕业发展和稳定的重大挑战。长链非编码 RNA(lncRNAs)已被报道在基因表达调控、发育和免疫反应中发挥重要作用,但 lncRNAs 在 BmNPV 感染和家蚕-BmNPV 相互作用中的作用尚不清楚。我们使用全基因组转录组分析来鉴定家蚕细胞(BmN 细胞)中的 lncRNAs,并分析了有无 BmNPV 感染时家蚕细胞中差异表达的 lncRNAs、microRNAs 和蛋白编码基因。在家蚕细胞中鉴定出了 13159 个候选 lncRNAs,其中 4450 个 lncRNAs 差异表达(DE),其中 2837 个上调,1613 个下调。此外,还鉴定出了 66 个差异表达的 microRNAs(DEmiRNAs)和 7448 个差异表达的 mRNAs(DEmRNAs),并构建了 DElncRNA-DEmiRNA-DEmRNA 调控网络。在 BmNPV 感染细胞中,预测的 lncRNA 顺式靶基因的 4973 个基因表达发生了变化。KEGG 通路分析表明,DElncRNA 靶基因富集在泛素介导的蛋白水解、内吞作用和溶酶体途径中。qRT-PCR 验证了几个 lncRNAs 和 miRNAs 的差异表达。我们的研究结果表明,DElncRNAs 通过与靶基因和 miRNAs 的相互作用参与宿主对 BmNPV 感染的反应。我们的研究结果将有助于我们提高对 lncRNA 介导的 BmNPV 感染调控作用的认识,并为家蚕-病原体相互作用提供新的见解。

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